Total Synthesis of Asperphenins A and B - ACS Publications

Sep 20, 2018 - State Key Laboratory of Chemical Oncogenomics, Key Laboratory of Chemical Genomics, Peking University Shenzhen Graduate. School, Xili ...
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Letter Cite This: Org. Lett. 2018, 20, 6170−6173

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Total Synthesis of Asperphenins A and B Jia-Lei Yan,† Yingying Cheng,† Jing Chen,† Ranjala Ratnayake,‡,§ Long H. Dang,‡,§,∥ Hendrik Luesch,‡,§ Yian Guo,*,† and Tao Ye*,† †

State Key Laboratory of Chemical Oncogenomics, Key Laboratory of Chemical Genomics, Peking University Shenzhen Graduate School, Xili, Nanshan District, Shenzhen 518055, China ‡ Department of Medicinal Chemistry, §Center for Natural Products, Drug Discovery and Development (CNPD3), and ∥Department of Medicine, University of Florida, Gainesville, Florida 32610, United States

Org. Lett. 2018.20:6170-6173. Downloaded from pubs.acs.org by UNIV OF SUNDERLAND on 10/05/18. For personal use only.

S Supporting Information *

ABSTRACT: The first total synthesis of asperphenins A and B has been accomplished in a concise, highly stereoselective fashion from commercially available materials (15 steps, 9.7% and 14.2% overall yields, respectively). The convergent route featured the judicious choice of protecting groups, fragment assembly strategy and a late-stage iron-catalyzed Wacker-type selective oxidation of an internal alkene to the corresponding ketone.

M

ments and ECD calculations. Structurally, these two natural products are composed of a β-hydroxy fatty acid, a tripeptide, and a trihydroxybenzophenone. Asperphenins A and B exhibit significant cytotoxicity against several human cancer cell lines, e.g., with IC50 values of 0.8 and 1.1 μM, respectively, against RKO colorectal carcinoma cells. Scheme 1 outlines our retrosynthetic analysis plan. We anticipated that the condensation of acid 3 with either fragment 4 or 5 followed by removal of protecting groups would give rise to the natural products. We envisioned the amine moiety of 4 or 5 could arise from either asymmetric Mannich reaction of ketone 6a or a stereoselective Wittig olefination of aldehyde 6b with a leucinol-derived triphenylphosphonium salt. Both 6a and 6b, in turn, could be accessed from a reaction of aryl iodide 8 with lactols 7a and 7b, respectively. The synthesis of fragment 3 commenced with the known compound 9,3 which underwent titanium tetrachloride mediated enantioselective aldol reaction with caprinaldehyde to provide 104 as a single diastereomer in 81% yield (Scheme 2). Protection of the resulting alcohol as its TBS ether followed by hydrolytic cleavage of the chiral auxiliary furnished the acid 11 in 76% yield. In parallel, coupling of N-Cbz-L-asparagine and L-glutamine methyl ester under the influence of HATU in the presence of HOAt and DIPEA furnished the corresponding dipeptide, which was subjected to hydrogenolysis of the Cbz protecting group to produce amine 14 in 76% yield over two steps. A second HATU/HOAt-mediated condensation of acid 11 and amine 14 provided the corresponding amide 15 in 85% yield. Saponification of the methyl ester with LiOH in aqueous methanol followed by acidification afforded the acid 3 in 81% yield.

etabolites isolated from marine fungus often possess unique structural features and incorporate new or unusual assemblages of functional groups. Many of them provide novel lead molecules for probing fundamental biological processes and the development of novel chemotherapeutic agents that target cancers. Our laboratory is engaged in a program devoted to the total synthesis and evaluation of marine natural products.1 Herein, we disclose the first total synthesis of asperphenins A and B by utilizing a highly efficient and convergent approach. Asperphenins A and B (Scheme 1) were isolated from a culture broth of marine-derived Aspergillus sp. collected from the shore of Jeju Island, Korea.2 The relative and absolute stereochemical configuration of asperphenins had been established by a combination of spectroscopic analyses, chemical degradation, Mosher ester analysis, CD measureScheme 1. Retrosynthetic Analysis of Asperphenin A

Received: August 19, 2018 Published: September 20, 2018 © 2018 American Chemical Society

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DOI: 10.1021/acs.orglett.8b02652 Org. Lett. 2018, 20, 6170−6173

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Organic Letters

corresponding lactol 7a as a latent hydroxyaldehyde in 95% yield. Spurred by Knochel’s seminal findings on halogen− magnesium exchange,7 we opted to convert the readily available aryl iodide 8 to the corresponding arylmetal species with i-PrMgCl·LiCl, followed by the addition of lactol 7a to give rise to biphenyl diol 21 as a mixture of diastereomers in 85% yield. Ley’s TPAP oxidation8 of 21 delivered the corresponding diketone 6a in 78% yield and set the stage for the exploration of the key asymmetric Mannich reaction.9 However, this reaction proved to be challenging due to the high propensity of trapping of the transient enolate intramolecularly with an electrophile. Accordingly, treatment of methyl ketone 6a and tert-butanesulfinyl imine 22 with various bases, solvents, and concentrations at low temperature resulted in no observation of the desired product. For example, exposure of both 6a and 22 in the presence of 1 equiv of potassium hexamethyldisilazane (KHMDS) provided two aldol products (23 and 24). Given that the reactions afforded βamino ketone 23 as the major product, we reasoned that the asymmetric Mannich reaction occurred with simultaneous cyclization of the regenerated enolate onto the ketone to afford the thermodynamically more stable product. To circumvent the problems encountered in the above strategy toward the construction of chiral amine 4 via an asymmetric Mannich reaction, we turned our attention to the strategy where the ketone moiety would have to be installed at a later stage of the synthesis. Thus, aldehyde 18 was transformed into lactone 25 by a two-step sequence involving (1) reduction with sodium borohydride and (2) acidpromoted lactonization. Lactone 25 was then elaborated to the lactol 7b in 81% yield by an identical strategy as described for 7a, including methyl ether deprotection and reprotection of the resulting free phenol with benzyl bromide and potassium carbonate, followed by partial reduction of the lactone with DIBAL-H at −78 °C. Again, the Grignard reagent derived from aryl iodide 8 added to lactol 7b provided biphenyl diol 27 in 72% yield. To our surprise, the use of the previously employed Ley’s TPAP oxidation of diol 27 led to the dicarbonyl product 6b in 27% yield along with the overoxidation product 28 (58%) (Scheme 4). Similar results were obtained with manganese dioxide11 in dichloromethane. 2,3Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ)12 oxidation of the benzylic alcohols in 27 provided intractable mixtures with

Scheme 2. Synthesis of Fragment 3

Our planned first approach to asperphenin A required the synthesis of fragment 4 from ketone 6a via an asymmetric Mannich reaction (Scheme 3). Thus, 2-methoxy-4-methylScheme 3. Attempts on the Synthesis of Intermediate 4

Scheme 4. Synthesis of Aldehyde 6b

benzoic acid 16 was converted into the corresponding acid chloride and then coupled with N,N-diethylamine to afford 17 in 95% yield. Regioselective formylation of 17 to aldehyde 18 was achieved through an amide-directed ortho-lithiation (tBuLi, TMEDA) and quenching with DMF (86% yield).5 Addition of methylmagnesium bromide to aldehyde 18 afforded the corresponding secondary alcohol, which was immediately subjected to acid-promoted lactonization to give rise to 19 in 92% yield over two steps.5b,6 Lactone 19 was treated with boron tribromide in dichloromethane to produce the crude deprotected phenol, which was then reprotected by benzylation using benzyl bromide and potassium carbonate to afford the benzyl derivative 20 in 81% yield. Partial reduction of the lactone 19 using DIBAL-H at −78 °C furnished the 6171

DOI: 10.1021/acs.orglett.8b02652 Org. Lett. 2018, 20, 6170−6173

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Organic Letters

entries 1−4). The literature precedents suggested that Wacker oxidation of cinnamyl azides17a and 2-styryltetrahydro-2Hpyrans17b occurred predominantly or exclusively at the benzylic rather than the homobenzylic carbon. Attempted Wacker oxidation of both 31 and 32, however, delivered only trace quantities of the desired ketone. As we searched for alternative methods of transforming alkenes 31 and 32 into ketones 33a and 33b, we were drawn to a report by Han and co-workers of a mild variant of the Wacker-type oxidation.18 In the Han’s modification of the Wacker oxidation, iron(II) chloride, polymethylhydrosiloxane, and air were employed as a highly efficient and selective catalytic system. Because the mild oxidation conditions enable exceptional functional-group tolerance, we tested this protocol with alkene 31. We were pleased to discover that the iron-catalyzed Wacker-type oxidation of alkene 31 provided ketone 33a in 30% yield. To our delight, the same iron-catalyzed aerobic oxidation of 32 delivered 33b in 89% yield (Table 1, entries 7 and 8). Encouraged by the successful transformation of alkene 32 to the corresponding β-ketone amide 33b, we proceeded with the total synthesis of asperphenin A and B as outlined in Schemes 6 and 7. Thus, coupling of acid 3 and allylic amine 5 under the

no desired products. Gratifyingly, treatment of diol 27 with PCC on alumina13 in DCM smoothly afforded the desired aldehyde 6b in 76% yield as the sole product. In parallel, D-leucinol (29) was transformed into trifluoroacetamide 30 by a three-step sequence involving (1) trifluoroacetylation of the primary amine, (2) conversion of the alcohol into the bromide with CBr4 and Ph3P, and (3) βamino phosphonium salt formation upon treating the resulting bromide with triphenylphosphine in refluxing toluene. Wittig reaction of aldehyde 6b with the phosphorane derived from phosphonium bromide 30 was next examined. Thus, treatment of the phosphonium salt 30 with 2.1 equiv of n-butyllithium followed by addition of the aldehyde 6b delivered the alkene 31 enriched in the desired E-isomer (E/Z = 5:1).14 The desired product 31 could be isolated free of the Z isomer in 77% yield by chromatography on silica gel. The presence of the trifluoroacetamide in 30 ensured the generation of the dianion intermediate, which presumably played a critical role to the stereochemical outcome of this transformation.14b,15 Hydrolysis of the trifluoroacetamide 31 gave allylic amine 5 in nearly quantitative yield. Acetylation of amine 5 was achieved under basic conditions with acetyl chloride to afford 32 in 82% yield (Scheme 5).

Scheme 6. Synthesis of Asperphenin A Scheme 5. Synthesis of Amine 5 and Amides 31 and 32

With alkenes 31 and 32 in hand, the stage was set to explore the crucial Wacker-type oxidation. Attempts to selectively oxidize the E-alkenes 31 and 32 using molecular iodine or Niodosuccinimide16 gave little or no desired products (Table 1,

Scheme 7. Synthesis of Asperphenin B

Table 1. Optimization of the Wacker-Type Oxidation

entry

alkene

condition

temp (°C)

yield (%)

1 2 3 4 5 6 7 8

31 32 31 32 31 32 31 32

I2, dioxane/H2O I2, dioxane/H2O NIS, dioxane/H2O NIS, dioxane/H2O PdCl2, CuCl, O2, H2O, DMF PdCl2, CuCl, O2, H2O, DMF FeCl2, PMHS, EtOH, air FeCl2, PMHS, EtOH, air

90 90 30 30 50 50 80 80

ND ND trace trace trace trace 30 89

influence of EDCI in the presence of HOAt and DIPEA afforded 34 in 71% yield. After removal of the TBS group to give rise to the corresponding alcohol 35, the alcohol was then subjected to an iron-catalyzed Wacker oxidation to furnish 36 in 85% yield. The final global hydrogenative debenzylation went on without incident to provide asperphenin A in 72% yield (Scheme 6). To this end, we synthesized ent-5 following the same synthesis as for 5, but starting with L-leucinol. This was readily achieved, and ent-5 was incorporated into the synthesis as previously performed to afford asperphenin B with no adverse consequences (Scheme 7). The spectral data for synthetic 1 and 2 (1H and 13C NMR and HMRS) were identical with those published for the natural products, and the optical rotation of our products ([α]D25 −22.0, c 0.1, MeOH, 6172

DOI: 10.1021/acs.orglett.8b02652 Org. Lett. 2018, 20, 6170−6173

Organic Letters



for asperphenin A; [α]D25 −16.2, c 0.1, MeOH, for asperphenin B) corresponded well with the literature value (lit.2 [α]D25 −24.7, c 0.1, MeOH, for asperphenin A; [α]D25 −18.4, c 0.1, MeOH, for asperphenin B), leading us to conclude that synthetic 1 and 2 were of the same absolute stereochemistry as natural asperphenins A and B. With the synthetic asperphenins A (1) and B (2) in hand, the screening of cytotoxic activities toward a number of cancer cell lines was investigated. The initial cytotoxicity evaluation of 1 and 2 was performed across a panel of the HIF-dependent HCT116 colorectal cancer cell lines using isogenic (HCT116HIF‑1α−/−HIF‑2α−/− and HCT116WT KRAS) knock-out cells to identify if these compounds preferentially target HIF/ KRAS pathways (Figure 1). Both compounds were only

ACKNOWLEDGMENTS We acknowledge financial support from the Shenzhen Peacock Plan (KQTD2015071714043444), the NSFC (21772009), the SZSTIC (JCYJ20160527100424909, JCYJ20170818090017617, JCYJ20170818090238288), the GDNSF (2014B030301003), the National Institutes of Health (NCI Grant No. R01CA172310), the Debbie and Sylvia DeSantis Chair professorship (H.L.), and the NCI Research Specialist Award (R50CA211487) (R.R.).



moderately cytotoxic against parental HCT116 with reduced cytotoxicity against the human normal colon cells, CCD18Co.10 Asperphenin A (1) shows a 2-fold decrease in potency against HCT116HIF‑1α−/−HIF2α−/− (IC50 shifts from 2.2 uM to 5.1 μM) with a simultaneous decrease in efficacy. For cells lacking oncogenic KRAS (HCT116WT KRAS), only a slight decrease in total efficacy was observed compared to the parental HCT116 cell line.10 Asperphenins may have a slight selectivity for colon cancer cells over normal cells that could be explored further with SAR studies. In summary, stereocontrolled total synthesis of asperphenins A and B has been accomplished through combination of a judicious choice of protecting groups, a fragment assembly strategy, and a late-stage iron-catalyzed Wacker-type selective oxidation of an internal alkene to the corresponding ketone. Both of the synthetic samples exhibit interesting results in the preliminary biological assays.

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S Supporting Information *

The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acs.orglett.8b02652. Experimental details and data (PDF)



REFERENCES

(1) (a) Al-Awadhi, F. H.; Gao, B.; Rezaei, M. A.; Kwan, J. C.; Li, C.; Ye, T.; Paul, V. J.; Luesch, H. J. Med. Chem. 2018, 61, 6364. (b) Guo, Y.; Zhao, M.; Xu, Z.; Ye, T. Chem. - Eur. J. 2017, 23, 3572. (c) Zhou, J.; Gao, B.; Xu, Z.; Ye, T. J. Am. Chem. Soc. 2016, 138, 6948. (d) Gunasekera, S. P.; Li, Y.; Ratnayake, R.; Luo, D.; Lo, J.; Reibenspies, J. H.; Xu, Z.; Clare-Salzler, M. J.; Ye, T.; Paul, V. J.; Luesch, H. Chem. - Eur. J. 2016, 22, 8158. (e) Qu, S.; Chen, Y.; Wang, X.; Chen, S.; Xu, Z.; Ye, T. Chem. Commun. 2015, 51, 2510. (f) Lei, H.; Yan, J.; Yu, J.; Liu, Y.; Wang, Z.; Xu, Z.; Ye, T. Angew. Chem., Int. Ed. 2014, 53, 6533. (2) Liao, L.; Bae, S. Y.; Won, T. H.; You, M.; Kim, S.-H.; Oh, D.-C.; Lee, S. K.; Oh, K.-B.; Shin, J. Org. Lett. 2017, 19, 2066. (3) Kitir, B.; Baldry, M.; Ingmer, H.; Olsen, C. A. Tetrahedron 2014, 70, 7721. (4) (a) Yadav, J. S.; Dachavaram, S. S.; Grée, R.; Das, S. Tetrahedron Lett. 2015, 56, 3999. (b) Yadav, J. S.; Rajendar, G.; Ganganna, B.; Srihari, P. Tetrahedron Lett. 2010, 51, 2154. (5) (a) Snieckus, V. Chem. Rev. 1990, 90, 879. (b) Li, Z.; Gao, Y.; Tang, Y.; Dai, M.; Wang, G.; Wang, Z.; Yang, Z. Org. Lett. 2008, 10, 3017. (6) Brimble, M. A.; Flowers, C. L.; Hutchinson, J. K.; Robinson, J. E.; Sidford, M. Tetrahedron 2005, 61, 10036. (7) (a) Knochel, P.; Dohle, W.; Gommermann, N.; Kneisel, F. F.; Kopp, F.; Korn, T.; Sapountzis, I.; Vu, V. A. Angew. Chem., Int. Ed. 2003, 42, 4302. (b) Krasovskiy, A.; Knochel, P. Angew. Chem., Int. Ed. 2004, 43, 3333. (c) Krasovskiy, A.; Straub, B. F.; Knochel, P. Angew. Chem., Int. Ed. 2006, 45, 159. (8) Saha, T.; Maitra, R.; Chattopadhyay, S. K. Beilstein J. Org. Chem. 2013, 9, 2910. (9) (a) Babij, N. R.; Wolfe, J. P. Angew. Chem., Int. Ed. 2012, 51, 4128. (b) Davis, F. A.; Yang, B. Org. Lett. 2003, 5, 5011. (c) Tang, T. P.; Ellman, J. A. J. Org. Chem. 2002, 67, 7819. (10) For details, see the Supporting Information. (11) (a) Hollinshead, S. P.; Nichols, J. B.; Wilson, J. W. J. Org. Chem. 1994, 59, 6703. (b) Srivastava, A. K.; Panda, G. Chem. - Eur. J. 2008, 14, 4675. (12) (a) Torricelli, F.; Bosson, J.; Besnard, C.; Chekini, M.; Bürgi, T.; Lacour, J. Angew. Chem., Int. Ed. 2013, 52, 1796. (b) Bosson, J.; Labrador, G. M.; Pascal, S.; Miannay, F.-A.; Yushchenko, O.; Li, H.; Bouffier, L.; Sojic, N.; Tovar, R. C.; Muller, G.; Jacquemin, D.; Laurent, A. D.; Le Guennic, B.; Vauthey, E.; Lacour, J. Chem. - Eur. J. 2016, 22, 18394. (13) Flanagan, S. R.; Harrowven, D. C.; Bradley, M. Tetrahedron 2002, 58, 5989. (14) (a) Andersson, I. E.; Dzhambazov, B.; Holmdahl, R.; Linusson, A.; Kihlberg, J. J. Med. Chem. 2007, 50, 5627. (b) Wiktelius, D.; Luthman, K. Org. Biomol. Chem. 2007, 5, 603. (15) Maryanoff, B. E.; Reitz, A. B.; Duhl-Emswiler, B. A. J. Am. Chem. Soc. 1985, 107, 217. (16) Harikrishna, K.; Mukkamala, R.; Hinkelmann, B.; Sasse, F.; Aidhen, I. S. Eur. J. Org. Chem. 2014, 2014, 1066. (17) (a) Carlson, A. S.; Calcanas, C.; Brunner, R. M.; Topczewski, J. Org. Lett. 2018, 20, 1604. (b) Keinan, E.; Seth, K. K.; Lamed, R. J. Am. Chem. Soc. 1986, 108, 3474. (18) (a) Liu, B.; Jin, F.; Wang, T.; Yuan, X.; Han, W. Angew. Chem., Int. Ed. 2017, 56, 12712. (b) Liu, B.; Han, W. Synlett 2018, 29, 383.

Figure 1. Effect of asperphenins A (1) and B (2) on isogenic HCT116 colon cancer cells and normal colon cells.



Letter

AUTHOR INFORMATION

Corresponding Authors

*E-mail: [email protected]. *E-mail: [email protected]. ORCID

Hendrik Luesch: 0000-0002-4091-7492 Yian Guo: 0000-0002-0341-6816 Tao Ye: 0000-0002-2780-9761 Notes

The authors declare no competing financial interest. 6173

DOI: 10.1021/acs.orglett.8b02652 Org. Lett. 2018, 20, 6170−6173